US1759660A - Production of pure iron - Google Patents

Production of pure iron Download PDF

Info

Publication number
US1759660A
US1759660A US203258A US20325827A US1759660A US 1759660 A US1759660 A US 1759660A US 203258 A US203258 A US 203258A US 20325827 A US20325827 A US 20325827A US 1759660 A US1759660 A US 1759660A
Authority
US
United States
Prior art keywords
iron
production
carbonyl
decomposition
pure iron
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US203258A
Inventor
Mittasch Alwin
Muller Carl
Linckh Eduard
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Application granted granted Critical
Publication of US1759660A publication Critical patent/US1759660A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B5/00General methods of reducing to metals
    • C22B5/02Dry methods smelting of sulfides or formation of mattes
    • C22B5/20Dry methods smelting of sulfides or formation of mattes from metal carbonyls

Definitions

  • pure iron can be produced from iron carbonyl by thermal decomposition by passing the iron carbonyl, in a vaporous and diluted condition, that is in the presence of inert or reducing gases or under diminished pressure, through heated liquids or melts.
  • the method according to the present invention is preferable to employing a' gas which dilutes the carbonyl vapor, since such gas extracts considerable quantities of heat in its passage through the melt
  • the decomposition of the iron carbonyl can be carried out for example by passing the liquid or vaporous carbonyl throu h the heated liquid or melt at ordnary or un er increased pressure, or by bringing it, in the form of vapor, into contact with the surface of a suitably agitated liquid or melt, or by spraying or dropping it, in the liquid condition, onto the liquid.
  • the working temperatures generally employed are between 100 and ,400" C or above 1000 C. in order to prevent extensive deposition of carbon as the result of the decomposition ofcarbon monoxid at the intermediate range of temperature. If, however, it is desired to obtain an iron possessing acertain high content of carbon or iron carbide, the decomposition is efi'ected'at temperatures between 400 and 1000 C
  • Organic liquids of high boiling point, such as paraffin oils and the like, have been found suitable substances for the decomposition process. Substances of lower boiling point may also be used, provided the operation be carried out in closed vessels under pressure.
  • the decomposition may also be effected with the aid of melts of salts or metals, in which case, according to the nature of the melt, the resulting iron is deposited either in the form of a fine powder, as when heated liquids are used, or is dissolved in the melt as, for ex ample, when the decomposition is eifected in molten iron, the metal being then produced directly in a pure, compact state.
  • the process according to the present in- "ention hasthe advantage that no gas is required for diluting the carbonyl, for which purposeno industrial gas can generally be employed, as such diluting gas must be dry and free from oxidizing constituents, so that it 1s rather expensive to produce. Moreover, by the absence of a diluting as a considera ly smaller supply of heat is necessary, as no gas mustbe heated together with the carbonyl. Further, in the present process pure carbon monoxid is recovered while in the operation with diluted iron carbonyl the carbon monoxid is strongly diluted with other gasesand therefore not suitable for all industrial purposes, unless pure carbon monoxid itself be employed as diluting gas.

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Patented May 20, 1930 UNITED STATES PATENT OFFICE ALWIN MITTASCH, AND CARL MNLLER, OF MANN HEIM, AND EDUARD LINC'KH, OF LUD- WIGSHAFEN-ON-THE-RHINE, GERMANY, ASSIGNORS TO I. G. FARBENINDUSTRIE AK- TIENGESELLSCHAFT, OF FRANKFORT-ON-THE-MAIN, GERMANY, A CORPORATION 01' GERILANY Io Drawing. Application filed July 2, 1927, Serial No. 203,258, and in Germany July 5, 1926.
It is known that pure iron can be produced from iron carbonyl by thermal decomposition by passing the iron carbonyl, in a vaporous and diluted condition, that is in the presence of inert or reducing gases or under diminished pressure, through heated liquids or melts. v
We have now found that it is not essential to employ the iron carbonyl in a diluted con dition, but that it is often preferable to bring it in an undiluted liquid or vaporous condition into contact wth the hot liquid" or melt. If, for example, the decomposition be effected by introducing iron carbonyl into molten iron, the method according to the present invention is preferable to employing a' gas which dilutes the carbonyl vapor, since such gas extracts considerable quantities of heat in its passage through the melt The decomposition of the iron carbonyl can be carried out for example by passing the liquid or vaporous carbonyl throu h the heated liquid or melt at ordnary or un er increased pressure, or by bringing it, in the form of vapor, into contact with the surface of a suitably agitated liquid or melt, or by spraying or dropping it, in the liquid condition, onto the liquid.
The working temperatures generally employed are between 100 and ,400" C or above 1000 C. in order to prevent extensive deposition of carbon as the result of the decomposition ofcarbon monoxid at the intermediate range of temperature. If, however, it is desired to obtain an iron possessing acertain high content of carbon or iron carbide, the decomposition is efi'ected'at temperatures between 400 and 1000 C Organic liquids of high boiling point, such as paraffin oils and the like, have been found suitable substances for the decomposition process. Substances of lower boiling point may also be used, provided the operation be carried out in closed vessels under pressure. The decomposition may also be effected with the aid of melts of salts or metals, in which case, according to the nature of the melt, the resulting iron is deposited either in the form of a fine powder, as when heated liquids are used, or is dissolved in the melt as, for ex ample, when the decomposition is eifected in molten iron, the metal being then produced directly in a pure, compact state.
The process according to the present in- "ention hasthe advantage that no gas is required for diluting the carbonyl, for which purposeno industrial gas can generally be employed, as such diluting gas must be dry and free from oxidizing constituents, so that it 1s rather expensive to produce. Moreover, by the absence of a diluting as a considera ly smaller supply of heat is necessary, as no gas mustbe heated together with the carbonyl. Further, in the present process pure carbon monoxid is recovered while in the operation with diluted iron carbonyl the carbon monoxid is strongly diluted with other gasesand therefore not suitable for all industrial purposes, unless pure carbon monoxid itself be employed as diluting gas.
The following example will further illustrate how the invention may be carried out in practice but the invention is not restricted thereto.
Ewample set our hands.
ALWIN MITTASCH. CARL MULLER. EDUARD. LINOKH.
US203258A 1926-07-05 1927-07-02 Production of pure iron Expired - Lifetime US1759660A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE1759660X 1926-07-05

Publications (1)

Publication Number Publication Date
US1759660A true US1759660A (en) 1930-05-20

Family

ID=7742127

Family Applications (1)

Application Number Title Priority Date Filing Date
US203258A Expired - Lifetime US1759660A (en) 1926-07-05 1927-07-02 Production of pure iron

Country Status (1)

Country Link
US (1) US1759660A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2612440A (en) * 1950-05-03 1952-09-30 Gen Aniline & Film Corp Production of metal carbonyl powders of small size

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2612440A (en) * 1950-05-03 1952-09-30 Gen Aniline & Film Corp Production of metal carbonyl powders of small size

Similar Documents

Publication Publication Date Title
DE69215345T2 (en) Treatment of synthesis gas
US2159077A (en) Production of valuable hydrocarbons and their derivatives containing oxygen
US1941809A (en) Art of hydrogenating and distilling oil shale
US1759660A (en) Production of pure iron
US1988781A (en) Process for preparing a mixture of nitrogen and hydrogen
US1562914A (en) Process for producing carbon and hydrocyanic acid
GB271452A (en) A process for the manufacture and production of hydrocarbons
US2094128A (en) Chemical process
US2389810A (en) Process for recovering elemental sulphur from sulphurous gases
US3397954A (en) Process for dehydrating boric acid
US2594149A (en) Sulfur recovery
US2594171A (en) Process for cooling hot gaseous suspensions of carbon black
US1765809A (en) Process of making carbon bisulphide
US1978069A (en) Producing diphenyl
US1375116A (en) Production of aluminum chlorid
US2385505A (en) Production of halides
US2487474A (en) Preparation of magnesium nitride
US1743740A (en) Method for making anhydrous zinc chloride by reacting zinc oxide with chlorine
US3019089A (en) Production of boron trichloride
US1415028A (en) Process for the treatment of ores of vanadium
US2162619A (en) Metallurgical process
US1360312A (en) Process of making carbonyl chlorid
US1614625A (en) Manufacture of iron carbonyl
US1712641A (en) Process for extracting metals from their compounds
US2311459A (en) Chlorination of chromium bearing materials